Abstract:Carbon dots (CDs) have gradually become a new generation of nano‐luminescent materials, which have received extensive attention due to excellent optical properties, wide source of raw materials, low toxicity, and good biocompatibility. In recent years, there are many reports on the luminescent phenomenon of CDs, and great progress has been achieved. However,there are rarely systematic summaries on CDs with persistent luminescence. Here, a summary of the recent progress on persistent luminescent CDs, including … Show more
“…Some CT states dissociate into CS states due to excimer complexes produced by photoexcitation, and the slow recombination of separated carriers leads to LPL (Figure 11b). [ 172 ]…”
Section: Other Solid‐state Luminescence Phenomenamentioning
confidence: 99%
“…Reproduced with permission. [ 172 ] Copyright 2023, Wiley‐VCH. c) CDs@Mn‐framework Composite design diagram.…”
Section: Other Solid‐state Luminescence Phenomenamentioning
confidence: 99%
“…The ideal band gap required for effective RISC to achieve TADF is less than 0.3 eV. [ 172 ] At present, CD‐based materials with TADF are constructed by dispersing the CDs into a substrate. A rigid substrate can form covalent or hydrogen bonds with the CDs, prevent oxygen quenching, protect and stabilize triplet excitons, and promote RISC.…”
Section: Other Solid‐state Luminescence Phenomenamentioning
Carbon dots (CDs)—carbon nanoparticles smaller than 10 nm—have attracted widespread attention owing to their excellent optical properties. However, high‐performing CDs often suffer from severe aggregation‐induced quenching in the solid state, which limits their commercial applicability. Therefore, CD materials with efficient solid‐state luminescence are sought. As research on the structure and photoluminescence mechanisms of CDs has intensified in recent years, strategies to construct fluorescent solid‐state CD materials and tune their emissions have broadened. This article reviews recent advances in the strategies and mechanisms for attaining solid‐state fluorescence in CDs, describes specific ways to tune the optical properties of this fluorescence, introduces the latest applications of the resulting CDs to optoelectronics, biology, and sensing, and finally considers the prospects for future application and current challenges facing the development of solid‐state fluorescence in CDs.
“…Some CT states dissociate into CS states due to excimer complexes produced by photoexcitation, and the slow recombination of separated carriers leads to LPL (Figure 11b). [ 172 ]…”
Section: Other Solid‐state Luminescence Phenomenamentioning
confidence: 99%
“…Reproduced with permission. [ 172 ] Copyright 2023, Wiley‐VCH. c) CDs@Mn‐framework Composite design diagram.…”
Section: Other Solid‐state Luminescence Phenomenamentioning
confidence: 99%
“…The ideal band gap required for effective RISC to achieve TADF is less than 0.3 eV. [ 172 ] At present, CD‐based materials with TADF are constructed by dispersing the CDs into a substrate. A rigid substrate can form covalent or hydrogen bonds with the CDs, prevent oxygen quenching, protect and stabilize triplet excitons, and promote RISC.…”
Section: Other Solid‐state Luminescence Phenomenamentioning
Carbon dots (CDs)—carbon nanoparticles smaller than 10 nm—have attracted widespread attention owing to their excellent optical properties. However, high‐performing CDs often suffer from severe aggregation‐induced quenching in the solid state, which limits their commercial applicability. Therefore, CD materials with efficient solid‐state luminescence are sought. As research on the structure and photoluminescence mechanisms of CDs has intensified in recent years, strategies to construct fluorescent solid‐state CD materials and tune their emissions have broadened. This article reviews recent advances in the strategies and mechanisms for attaining solid‐state fluorescence in CDs, describes specific ways to tune the optical properties of this fluorescence, introduces the latest applications of the resulting CDs to optoelectronics, biology, and sensing, and finally considers the prospects for future application and current challenges facing the development of solid‐state fluorescence in CDs.
“…However, most CDs-based RTP materials only present phosphorescence in their dry state, which tends to quench in aqueous solution . This is not only due to the destroy of the hydrogen-bond skeleton by the water molecules but also the triplet state of the CDs is affected by the presence of dissolved oxygen in the aqueous solution, leading to the quench of the phosphorescence . Gao et al obtained M-CDs by reacting CDs with melamine, which exhibited phosphorescence in solution due to the construction of the hydrogen bonding network structure .…”
Section: Introductionmentioning
confidence: 99%
“…15 This is not only due to the destroy of the hydrogen-bond skeleton by the water molecules but also the triplet state of the CDs is affected by the presence of dissolved oxygen in the aqueous solution, leading to the quench of the phosphorescence. 16 Gao et al obtained M-CDs by reacting CDs with melamine, which exhibited phosphorescence in solution due to the construction of the hydrogen bonding network structure. 17 Song et al synthesized yellow RTP-CDs using a mixture of 1,2,4-triaminobenzene, magnesium salt, and phosphate.…”
Room-temperature phosphorescence (RTP) plays an important
role
in the field of information encryption due to its ability to effectively
eliminate interference caused by background fluorescence (FL). Herein,
a series of RTP carbon dots (CDs) containing different nitrogen contents
were prepared via a molten salt method. In the reaction system, magnesium
chloride and potassium nitrate were used as doping salts to form salt
shells, and potassium nitrate was used as salt medium to promote the
reaction. By adjusting the amount of melamine, the synthesized CDs-3
exhibit cyan FL and yellow phosphorescence, with a long phosphorescence
lifetime of 673.29 ms. It is worth noting that the yellow RTP can
be maintained either in dry or wet state, which facilitates for the
information encryption. It is suggested that the salt shell composed
of magnesium salt with high charge density has a rigid structure,
which inhibits the nonradiative transition process of the triplet-state
exciton and enhances the phosphorescence intensity. Unfortunately,
when the amount of melamine increases to a certain extent, due to
the incomplete encapsulation of the salt shell, the phosphorescence
of the prepared CDs quenches accordingly. In addition, CDs-3 can also
be mixed with epoxy resin to obtain the desired fluorescent/phosphorescent
composites. These excellent optical properties indicate that the synthesized
CD materials have great development prospects in fields such as anti-counterfeiting
and luminescent materials.
Room temperature phosphorescent carbon dots (RTP CDs) have received increasing attention in recent years due to their outstanding optical properties and potential applications. It is worth noting that RTP CDs in aqueous solution have inspired special interests because of their low toxicity, long lifetime, and ability to avoid autofluorescence and background fluorescence, exhibiting wide application prospects in time‐resolved biological imaging and sensing. However, achieving phosphorescent CDs in aqueous solutions remains a considerable challenge because water molecules and oxygen can cause the deactivation of triplet‐state excitons, resulting in phosphorescence quenching. Several strategies have been proposed to counter the problem including encapsulated CDs in a rigid matrix, hydrogen bonding, and covalent bonding fixation. Consequently, a more significant number of RTP CDs materials with excellent optical stability, long lifetime, and multicolor are successfully obtained. Herein, the recent development of RTP CDs materials in aqueous solution as well as the corresponding fabricated strategies and luminescence mechanism is detailly summarized and reviewed. Furthermore, various applications of water‐phase RTP CDs materials in information security, sensing, bioimaging, light‐emitting diodes, and fingerprinting are also discussed. Finally, an outlook on the development of CDs materials and applications is proposed.
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